Browsing by Author "Nath, Avindra"

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    Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndrome
    (BRAIN, 2023) Soldatos, Ariane; Nutman, Thomas B.; Johnson, Tory; Dowell, Scott F.; Sejvar, James J.; Wilson, Michael R.; DeRisi, Joseph L.; Inati, Sara K.; Groden, Catherine; Evans, Colleen; O’Connell, Elise M.; Toliva, Bernard Opar; Aceng, Jane R.; Aryek-Kwe, Josephine; Toro, Camilo; Stratakis, Constantine A.; Buckler, A. Gretchen; Cantilena, Cathy; . Palmore, Tara N; Thurm, Audrey; Baker, Eva H.; Chang, Richard; Fauni, Harper; Adams, David; Macnamara, Ellen F.; Lau, C. Christopher; . Malicdan, May Christine V; Pusey-Swerdzewski, Barbara; Downing, Robert; Bunga, Sudhir; Thomas, Jerry D.; Gahl, William A.; Nath, Avindra
    https://doi.org/10.1093/brain/awac357 BRAIN 2023: 146; 968–976 | 968 Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndrome Ariane Soldatos,1 Thomas B. Nutman, 1 Tory Johnson,1 Scott F. Dowell,2 James J. Sejvar, 2 Michael R. Wilson,3,4 Joseph L. DeRisi, 3,5 Sara K. Inati, 1 Catherine Groden, 1 Colleen Evans, 1 Elise M. O’Connell, 1 Bernard Opar Toliva, 6 Jane R. Aceng,6 Josephine Aryek-Kwe, 6 Camilo Toro, 1 Constantine A. Stratakis, 1 A. Gretchen Buckler, 1 Cathy Cantilena,1 Tara N. Palmore,1 Audrey Thurm, 1 Eva H. Baker, 1 Richard Chang, 1 Harper Fauni, 1 David Adams, 1 Ellen F. Macnamara, 1 C. Christopher Lau, 1 May Christine V. Malicdan,1 Barbara Pusey-Swerdzewski, 1 Robert Downing,7 Sudhir Bunga,2 Jerry D. Thomas, 8 William A. Gahl1 and Avindra Nath 1 The aetiology of nodding syndrome remains unclear, and comprehensive genotyping and phenotyping data from pa- tients remain sparse. Our objectives were to characterize the phenotype of patients with nodding syndrome, inves- tigate potential contributors to disease aetiology, and evaluate response to immunotherapy. This cohort study investigated members of a single-family unit from Lamwo District, Uganda. The participants for this study were selected by the Ugandan Ministry of Health as representative for nodding syndrome and with a con- ducive family structure for genomic analyses. Of the eight family members who participated in the study at the National Institutes of Health (NIH) Clinical Center, three had nodding syndrome. The three affected patients were extensively evaluated with metagenomic sequencing for infectious pathogens, exome sequencing, spinal fluid immune analyses, neurometabolic and toxicology testing, continuous electroenceph- alography and neuroimaging. Five unaffected family members underwent a subset of testing for comparison. A dis- tinctive interictal pattern of sleep-activated bursts of generalized and multifocal epileptiform discharges and slowing was observed in two patients. Brain imaging showed two patients had mild generalized cerebral atrophy, and both patients and unaffected family members had excessive metal deposition in the basal ganglia. Trace metal biochem- ical evaluation was normal. CSF was non-inflammatory and one patient had CSF-restricted oligoclonal bands. Onchocerca volvulus-specific antibodies were present in all patients and skin snips were negative for active onchocer- ciasis. Metagenomic sequencing of serum and CSF revealed hepatitis B virus in the serum of one patient. Vitamin B6 metabolites were borderline low in all family members and CSF pyridoxine metabolites were normal. Mitochondrial DNA testing was normal. Exome sequencing did not identify potentially causal candidate gene variants. Nodding syndrome is characterized by a distinctive pattern of sleep-activated epileptiform activity. The associated growth stunting may be due to hypothalamic dysfunction. Extensive testing years after disease onset did not clarify a causal aetiology. A trial of immunomodulation (plasmapheresis in two patients and intravenous immunoglobulin in one patient) was given without short-term effect, but longer-term follow-up was not possible to fully assess any benefit of this intervention.
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    Neuroinflammation and Not Tauopathy Is a Predominant Pathological Signature of Nodding Syndrome
    (Journal of Neuropathology & Experimental Neurology, 2019) Hotterbeekx, An; Lammens, Martin; Idro, Richard; Akun, Pamela R.; Lukande, Robert; Akena, Geoffrey; Nath, Avindra; Taylor, Jonee; Olwa, Francis; Kumar-Singh, Samir; Colebunders, Robert
    Nodding syndrome (NS) is an epileptic disorder occurring in chil dren in African onchocerciasis endemic regions. Here, we describe the pathological changes in 9 individuals from northern Uganda who died with NS (n ¼ 5) or other forms of onchocerciasis-associated ep ilepsy (OAE) (n ¼ 4). Postmortem examinations were performed and clinical information was obtained. Formalin-fixed brain samples were stained by hematoxylin and eosin and immunohistochemistry was used to stain astrocytes (GFAP), macrophages (CD68), ubiqui tin, a-synuclein, p62, TDP-43, amyloid b, and tau (AT8). The cere bellum showed atrophy and loss of Purkinje cells with hyperplasia of the Bergmann glia. Gliosis and features of past ventriculitis and/ or meningitis were observed in all but 1 participant. CD68-positive macrophage clusters were observed in all cases in various degrees. Immunohistochemistry for amyloid b, a-synuclein, or TDP-43 was negative. Mild to sparse AT8-positive neurofibrillary tangle-like structures and threads were observed in 4/5 NS and 2/4 OAE cases, preferentially in the frontal and parietal cortex, thalamic- and hypo thalamic regions, mesencephalon and corpus callosum. Persons who died with NS and other forms of OAE presented similar pathological changes but no generalized tauopathy, suggesting that NS and other forms of OAE are different clinical presentations of a same disease with a common etiology. Key Words: Epilepsy, Nodding syndrome, Onchocerciasis, Post-mortem, Uganda.